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Endocrine Research|June 22, 2023
T Cell Subsets are Associated with Clinical Activity and Efficacy of 4.5g Intravenous Glucocorticoid for Moderate-To-Severe Thyroid-Associated OphthalmopathyHuixia Li, Bin Wang, Qin Li, et al.
Clinical and Translational Science|March 20, 2021
Influence of 4-week or 12-week glucocorticoid treatment on metabolic changes in patients with active moderate-to-severe thyroid-associated ophthalmopathyXiaoman Chen, Buatikamu Abudukerimu, Qin Li, et al.
American Journal of Respiratory and Critical Care Medicine|December 7, 2018
Identification and Modulation of Microenvironment Is Crucial for Effective Mesenchymal Stromal Cell Therapy in Acute Lung InjuryDiana Islam, Yongbo Huang, Vito Fanelli, et al.
Neuron|March 17, 2026
Oligodendrocyte-encoded lactate dehydrogenase A couples glycolysis to remyelination via protein lactylationMing-Yue Bao, Xiu-Qing Li, Qing-Qing Sun, et al.
Annals of Noninvasive Electrocardiology : the Official Journal of the International Society for Holter and Noninvasive Electrocardiology, Inc|July 26, 2021
The association between ECG criteria and Echo criteria for left ventricular hypertrophy in a general Chinese populationTingting Lv, Yifang Yuan, Jing Yang, et al.
Acta Haematologica|October 19, 2017
Very-Low-Dose Decitabine Is Effective in Treating Intermediate- or High-Risk Myelodysplastic SyndromeHongmin Li, Liru Wang, Yue Wu, et al.
Aging Cell|June 16, 2025
Chronic Cellular NAD Depletion Activates a Viral Infection-Like Interferon Response Through Mitochondrial DNA LeakageClaudia C S Chini, Laura Colman, Eduardo Palmieri, et al.
Mitochondrion|July 22, 2008
Mutations at position 7445 in the precursor of mitochondrial tRNA(Ser(UCN)) gene in three maternal Chinese pedigrees with sensorineural hearing lossJing Chen, Huijun Yuan, Jianxin Lu, et al.
Human Mutation|June 25, 2009
A splice site mutation combined with a novel missense mutation of LHCGR cause male pseudohermaphroditismJie Qiao, Bing Han, Bing-Li Liu, et al.
Molecular Genetics & Genomic Medicine|April 11, 2019
Prevalence of BRCA1 and BRCA2 gene mutations in Chinese patients with high-risk breast cancerXiaozhen Wang, Haimeng Liu, Amina Maimaitiaili, et al.
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